chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	16016287	16016288	G	A	9	GENIC	possibly homozygous	50502603
12	16016426	16016427	T	C	9	GENIC	homozygous	50076243
12	16017702	16017703	C	T	15	GENIC	homozygous	50502605
12	16019679	16019680	C	A	16	GENIC	possibly homozygous	50502606
12	16020255	16020256	T	C	23	GENIC	homozygous	50076250
12	16020607	16020608	C	T	24	GENIC	homozygous	50502607
12	16020796	16020797	C	T	18	GENIC	homozygous	50502608
12	16020819	16020820	C	T	23	GENIC	homozygous	50502609
12	16020974	16020975	A	T	24	GENIC	homozygous	50076256
12	16021182	16021183	G	A	10	GENIC	possibly homozygous	50076258
12	16021286	16021287	T	G	20	GENIC	heterozygous	50076260
12	16022336	16022337	A	C	12	GENIC	heterozygous	50076262
12	16023463	16023464	C	T	2	GENIC	homozygous	50502610
12	16023486	16023487	A	T	1	GENIC	homozygous	50076272
12	16023521	16023522	A	G	3	GENIC	homozygous	50502611
12	16024297	16024298	C	G	16	GENIC	homozygous	50502612
12	16024423	16024424	A	G	16	GENIC	homozygous	50076284
12	16026015	16026016	T	C	25	INTERGENIC	homozygous	50076294
12	16026345	16026346	G	A	24	INTERGENIC	possibly homozygous	50502613
12	16027684	16027685	C	T	11	INTERGENIC	homozygous	50502614